HG Awareness Month

Join the HER Foundation as we shed light on HG Truths all month long. Get INVOLVED SHARE your HG story. MEET other HG survivors on Zoom. FUNDRAISE for HG education & research. CHOOSE a Facebook frame for your profile. Search frames: hyperemesis HER Foundation. USE the hashtags on your social: #HGAM21 #HGAD21 #HGtruths. INVITE others to follow…

Read More

The Hearts of Gold HG Bracelet

Help us spread awareness by showing your #HGstyle everywhere you go! The Hearts of Gold gives back 10% of proceeds for this bracelet to HER Foundation.

Read More

HG Patient Cards & Logo Stickers or Cling Decal

These little business-sized cards are great to buy and share with those facing HG. On one side, they can find a list of resources HER offers women in need. On the back, there is a quick reference guide to HG treatment. Share them with others and educate them on HG care. We have durable full-color…

Read More

Global Partnerships Continue to Grow

In partnership with HG Indonesia and Orami Parenting, the HER Foundation presented about hyperemesis gravidarum (HG) for mothers in Indonesia. Indonesian mothers joined the live event where Kimber MacGibbon spoke and answered questions about HG. Petty Fathia, Co-founder of HG Indonesia, translated the presentation. Our work to educate and support women across the globe continues…

Read More

Losing Quinn

This time last year, I noticed Facebook friends posting about National Pregnancy and Infant Loss Awareness Day, a day I’d never heard of, and I made a note to hold space for those expectant parents who lost their babies. Three days later, I started bleeding and was devastated to learn that my 7 week embryo…

Read More

We hold them in our hearts

October is Pregnancy and Infant Loss (PAIL) Awareness Month, and we want to honor the memories of the little ones we hold in their hearts. October is Pregnancy and Infant Loss (PAIL) Awareness Month, and we want to honor the memories of the little ones we hold in their hearts. We are grateful for the transparency and love shared by members of our loss community.

Read More

HERstory: Saloni

For the second installment of the #HERstory Global Initiative, we spoke with Hyperemesis Gravidarum (HG) survivor Saloni, who is currently residing in India. She shed some light on her personal HG journey, which she is still undergoing to this day as she continues to recover. Because she believes that there is little HG awareness in…

Read More

HER Foundation is an Ambassador for Malnutrition Awareness Week

We are proud to announce that the HER Foundation has joined ASPEN, the American Society for Parenteral and Enteral Nutrition, as an Ambassador for ASPEN Malnutrition Awareness Week on October 5-9, 2020. It’s a week filled with valuable educational webinars and sharing of informational materials. The goal of Malnutrition Awareness Week is to educate healthcare…

Read More

Courtney shares about attending Champions for Change Summit in 2019

Words can’t describe the total shock and awe I felt at the Champions for Change Summit I attended on behalf of the HER Foundation, October 18-20, 2019. For years, I believed that women were either sick like me, specifically with Hyperemesis Gravidarum (HG), or that they must have had a wonderful pregnancy. My time at the Summit…

Read More

HERstory: Veronica

This summer, we had the pleasure of interviewing Veronica about her experience with Hyperemesis Gravidarum (HG). Veronica is an HG survivor and native Venezuelan who is currently residing in Toronto, Canada. Veronica is the first mom we were able to interview in her native language, Spanish, as part of our #HERstory Global Initiative. Below is…

Read More